Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas-Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine N'Guyen, Anne De Septenville, Alexis Brice, Patrick Yu-Wai-ManHiromi Sesaki, Jean Pouget, Véronique Paquis-Flucklinger

Research output: Contribution to journal › Article

Original languageEnglish (US)
Pages (from-to)e377
JournalBrain
Volume138
Issue number9
DOIs
StatePublished - Sep 1 2015

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Frontotemporal Dementia
Mitochondrial Diseases
Motor Neuron Disease
Mitochondrial Proteins
Amyotrophic Lateral Sclerosis
Mitochondrial DNA
Mitochondria
Phenotype
Mutation
Neuron

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Bannwarth, S., Ait-El-Mkadem, S., Chaussenot, A., Genin, E. C., Lacas-Gervais, S., Fragaki, K., ... Paquis-Flucklinger, V. (2015). Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Brain, 138(9), e377. https://doi.org/10.1093/brain/awv015

Reply : A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. / Bannwarth, Sylvie; Ait-El-Mkadem, Samira; Chaussenot, Annabelle; Genin, Emmanuelle C.; Lacas-Gervais, Sandra; Fragaki, Konstantina; Berg-Alonso, Laetitia; Kageyama, Yusuke; Serre, Valérie; Moore, David; Verschueren, Annie; Rouzier, Cécile; Le Ber, Isabelle; Augé, Gaëlle; Cochaud, Charlotte; Lespinasse, Françoise; N'Guyen, Karine; De Septenville, Anne; Brice, Alexis; Yu-Wai-Man, Patrick; Sesaki, Hiromi; Pouget, Jean; Paquis-Flucklinger, Véronique.

In: Brain, Vol. 138, No. 9, 01.09.2015, p. e377.

Research output: Contribution to journal › Article

Bannwarth, S, Ait-El-Mkadem, S, Chaussenot, A, Genin, EC, Lacas-Gervais, S, Fragaki, K, Berg-Alonso, L, Kageyama, Y, Serre, V, Moore, D, Verschueren, A, Rouzier, C, Le Ber, I, Augé, G, Cochaud, C, Lespinasse, F, N'Guyen, K, De Septenville, A, Brice, A, Yu-Wai-Man, P, Sesaki, H, Pouget, J & Paquis-Flucklinger, V 2015, 'Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation', Brain, vol. 138, no. 9, pp. e377. https://doi.org/10.1093/brain/awv015
Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K et al. Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. Brain. 2015 Sep 1;138(9):e377. https://doi.org/10.1093/brain/awv015
Bannwarth, Sylvie ; Ait-El-Mkadem, Samira ; Chaussenot, Annabelle ; Genin, Emmanuelle C. ; Lacas-Gervais, Sandra ; Fragaki, Konstantina ; Berg-Alonso, Laetitia ; Kageyama, Yusuke ; Serre, Valérie ; Moore, David ; Verschueren, Annie ; Rouzier, Cécile ; Le Ber, Isabelle ; Augé, Gaëlle ; Cochaud, Charlotte ; Lespinasse, Françoise ; N'Guyen, Karine ; De Septenville, Anne ; Brice, Alexis ; Yu-Wai-Man, Patrick ; Sesaki, Hiromi ; Pouget, Jean ; Paquis-Flucklinger, Véronique. / Reply : A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation. In: Brain. 2015 ; Vol. 138, No. 9. pp. e377.
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